Disease table

A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

Disease phenotype
OMIM
Gene symbol (chromosome)
protein
Thyrotoxic periodic paralysis, susceptibility to, 2 (7.13)
KCNJ18 (17p11.2)
Kir2.6 (inwardly rectifying potassium channel 2.6)

Tibial muscular dystrophy, tardive (5.13, 4.2, 1.28, 10.33, 10.8, 3.31)
TTN (2q31)
titin

Timothy syndrome (10.94, 10.113)
CACNA1C (12p13.3)
calcium channel, voltage-dependent, L type, alpha 1C subunit

Torsion dystonia, early onset (16.1)
TOR1A (9q34)
torsin A